Positionally ordered
bilayer liquid crystalline nanostructures
formed by gapped DNA (GDNA) constructs provide a practical window
into DNA–DNA interactions at physiologically relevant DNA concentrations;
concentrations several orders of magnitude greater than those in commonly
used biophysical assays. The bilayer structure of these states of
matter is stabilized by end-to-end base stacking interactions; moreover,
such interactions also promote in-plane positional ordering of duplexes
that are separated from each other by less than twice the duplex diameter.
The end-to-end stacked as well as in-plane ordered duplexes exhibit
distinct signatures when studied via small-angle X-ray scattering
(SAXS). This enables analysis of the thermal stability of both the
end-to-end and side-by-side interactions. We performed synchrotron
SAXS experiments over a temperature range of 5–65 °C on
GDNA constructs that differ only by the terminal base-pairs at the
blunt duplex ends, resulting in identical side-by-side interactions,
while end-to-end base stacking interactions are varied. Our key finding
is that bilayers formed by constructs with GC termination transition
into the monolayer state at temperatures as much as 30 °C higher
than for those with AT termination, while mixed (AT/GC) terminations
have intermediate stability. By modeling the bilayer melting in terms
of a temperature-dependent reduction in the average fraction of end-to-end
paired duplexes, we estimate the stacking free energies in DNA solutions
of physiologically relevant concentrations. The free-energies thereby
determined are generally smaller than those reported in single-molecule
studies, which might reflect the elevated DNA concentrations in our
studies.